Quality Control Reviewer

2 semanas atrás

Loures, Portugal Hovione Tempo inteiro

Join a Market Leader:
Hovione is an independent family owned international group of companies. From the beginning, we have set ourselves above and apart through our innovative technological and productive capabilities, reaching a top spot in the world market as an integrated Contract Development and Manufacturing Company dedicated to helping Pharmaceutical Customers bring new and off-patent drugs to market.

Our people are the main asset for our continued success. Reaching over 1950 team members, from 36 different nationalities, that are located across Asia, Europe and North America (Portugal, US, Macao, Ireland, China, Hong Kong, Japan, India, and Switzerland), including 4 production sites.

Working at Hovione means reaching for innovation and excellence in everything we do: for our clients, our partners and, above all, our patients. **That is why we are In it for life.**

You will be responsible to:

- Solve analytical problems relating to assigned projects by providing collaborative and timely support to all areas and departments;
- Ensure the effective and proactive flow of information between the Analytical team and the internal and external (if applicable) stakeholders, representing the team (with support from senior colleagues) as appropriate;
- Reviews work generated by the team as required ensuring all procedures are followed;
- Creation, investigation and evaluation of CAPAS, incidents and deviations;
- Perform equipment maintenance, internal calibrations and internal qualifications on designated laboratory instruments;
- Accurately use and maintain all laboratory information systems;
- Fulfil and promote all applicable GMP requirements and HSE regulations, adhering to all relevant Operating Procedures and industry standards in conducting all analytical activities;
- Assist with audits / investigations as required, following the instruction of QC Management;
- Support the reporting of KPIs for the team, if required;
- Use analytical techniques and instrumentation, such as gas and high-performance liquid chromatography (HPLC) amongst others;
- Interpretation of data and analysis to ensure meeting strict guidelines on documentation and recording data;
- University, or equivalent, qualification in Chemistry, Chemical Engineering, Pharmaceutical Sciences or similar Chemistry, Biochemistry or Health Sciences field (mandatory);
- Requires educational / training experience in a QC laboratory environment;
- Hands-on experience in Analytical Chemistry and QC procedures (desirable);
- Training and experience of GMP and ICH guidelines standards (desirable);
- Knowledge on HPLC and GC, and familiarity with Empower Software (mandatory);
- Technical understanding of GMP practices, analytical theory and techniques;
- Fluency in English is a requirement

**Hovione is a proud Equal Opportunity Employer**

Inclusion and diversity are key to us. At Hovione, that means a work environment where differences are valued, and everyone is treated with fairness and respect. We want all our team members worldwide to feel supported, respected, and have the opportunity to achieve their full potential, regardless of their age, gender, religion, disability, sexual orientation or ethnicity.

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